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SPF 30 Sunscreen
SPF 30 Sunscreen - 76138-203-09 - (OCTINOXATE, OXYBENZONE, OCTISALATE)
Drug Information of SPF 30 Sunscreen
| Product NDC: | 76138-203 |
| Proprietary Name: | SPF 30 Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE |
| Active Ingredient(s): | 7.5; 1; 4 g/100mL; g/100mL; g/100mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPF 30 Sunscreen
| Product NDC: | 76138-203 |
| Labeler Name: | INNOVATION SPECIALTIES |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121001 |
Package Information of SPF 30 Sunscreen
| Package NDC: | 76138-203-09 |
| Package Description: | 65 mL in 1 BOTTLE (76138-203-09) |
NDC Information of SPF 30 Sunscreen
| NDC Code | 76138-203-09 |
| Proprietary Name | SPF 30 Sunscreen |
| Package Description | 65 mL in 1 BOTTLE (76138-203-09) |
| Product NDC | 76138-203 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | INNOVATION SPECIALTIES |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.5; 1; 4 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
